Abstract 15432: Observation of Aortic Dilatation in Congenital Conotruncal Anomalies - Tetralogy of Fallot, Double Outlet Right Ventricle and Truncus Arteriosus

Circulation ◽  
2020 ◽  
Vol 142 (Suppl_3) ◽  
Author(s):  
Woojung Kim ◽  
Jae Gun Kwak

Backgrounds: Dilatation of aortic root or ascending aorta is often seen in the patients with conotruncal anomalies (CA). How fast these structures dilate and how we manage this phenomenon are not clear. Methods: We reviewed medical records of patients who underwent biventricular repair of CA such as tetralogy of Fallot (TOF), double outlet right ventricle (DORV) and truncus arteriosus (TA) from 2004 to 2018. We included 99 patients who had follow-up cardiac computed tomography angiography (CT) images at least 5 years since initial CT in this study. We analyzed changes of diameters of aortic root structures and ascending aorta between initial and follow-up CT images. Results: Median follow-up duration was 16.1 years (interquartile range (IQR): 11.8~26.2 years) after operation. Median interval between initial and follow-up CT examination was 9.4 years (IQR: 7.1~11.5 years). Median age of initial and follow-up CT was 4.3 years (IQR: 0.3~12.3 years) and 14.4 years (IQR: 9.2~22.9 years). The median z-scores (with IQR) of sinus of Valsalva (SV, 2.0 (0.8~3.3) → 2.4 (1.4~3.3), p=0.006) and sinotubular junction (STJ, 1.3 (-0.2~2.6) → 2.2 (0.4~3.3), p=0.001) were significantly changed, whereas aortic annulus (AA, 2.4 (0.9~3.4) → 2.3 (0.8~3.3), p=0.21) and ascending aorta (AsA, 1.6 (0.4~2.9) → 1.6 (0.03~2.6), p=0.27) did not show significant changes in CT images. Median increasing rate of diameter of AA, SV, STJ and AsA was 0.72, 0.93, 0.83 and 0.51 mm/year, respectively. Dilatation rate of AA (0.69 in TOF vs. 0.99 in TA, p=0.042) and SV (0.81 in TOF vs. 1.53 in TA, p=0.008) of TA was significantly higher than of TOF. Conclusions: In TOF, DORV and TA, SV and STJ significantly dilated, whereas AsA and AA did not significantly dilated for 9 years of follow-up. Although chance of surgical intervention for dilatation of aortic structures was rare, it might be necessary to observe closely aortic valvular function associated with structural deterioration of SV or STJ.

2017 ◽  
Vol 11 (4) ◽  
pp. NP94-NP98 ◽  
Author(s):  
Ashish Katewa ◽  
Balswaroop Sahu ◽  
Vishal Jain ◽  
Robert H. Anderson

We present a case of a highly unusual congenital cardiac malformation, namely, triple outlet right ventricle with duplication of the aortic root and the intrapericardial component of the ascending aorta. A girl, aged five, presented with complaints of cyanosis and effort intolerance and was diagnosed with double-outlet right ventricle and subpulmonary infundibular stenosis. Intraoperatively, we noted that the aortic root was guarded by two separate aortic valves, oriented anteroposteriorly relative to each other, and separated within the right ventricle by a muscle bar. Postoperative interrogation by both echocardiography and computed tomography confirmed the surgical findings. To the best of our knowledge, our case is the first example of duplication of the aortic root to produce triple outlet right ventricle.


2021 ◽  
Vol 8 ◽  
pp. 100354
Author(s):  
Suvipaporn Siripornpitak ◽  
Apichaya Sriprachyakul ◽  
Saruntorn Wongmetta ◽  
Piya Samankatiwat ◽  
Pirapat Mokarapong ◽  
...  

2019 ◽  
Author(s):  
D. Wagner ◽  
C. Gall ◽  
A. Rüffer ◽  
A. Purbojo ◽  
S. Dittrich ◽  
...  

1997 ◽  
Vol 5 (4) ◽  
pp. 247-249
Author(s):  
Fatih İslamoğlu ◽  
Yüksel Atay ◽  
İlker Alat ◽  
Osman Saribülbül ◽  
E Alp Alayunt

A 3-year-old female presented with double-outlet right ventricle associated with supravalvular mitral ring, parachute mitral valve, left persistent superior vena cava, and atrial septal defect. The supra-annular mitral valve ring was resected. Only one papillary muscle of the mitral valve could be detected and this was minimally divided to achieve adequate valve opening. An intraventricular tunnel repair technique using a polytetrafluoroethylene patch was carried out to repair the double-outlet right ventricle, which had a subaortic ventricular septal defect. The follow-up results at 2 years are excellent.


2007 ◽  
Vol 167 (1) ◽  
pp. 103-105 ◽  
Author(s):  
Junji Takaya ◽  
Naoyuki Kitamura ◽  
Kimiko Tsuji ◽  
Kentaro Watanabe ◽  
Yo Kinoshita ◽  
...  

Circulation ◽  
2005 ◽  
Vol 112 (7) ◽  
pp. 961-968 ◽  
Author(s):  
J.L. Tan ◽  
P.A. Davlouros ◽  
K.P. McCarthy ◽  
M.A. Gatzoulis ◽  
S.Y. Ho

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